Stay Informed

Get email alerts when new recalls match your interests.

Recall data is updated hourly from official government sources. Very recent recalls may not yet appear. About our data sources

About

We make U.S. recall data searchable and accessible for consumers and businesses.

Site

FAQ
Browse by State
Statistics
Recall Classifications
About
Enterprise API

Legal

Privacy Policy
Terms of Service
Report Incorrect Info

Official Sources

FDA Recalls ↗
USDA FSIS ↗
CPSC Recalls ↗
NHTSA Recalls ↗

RSS Feed

Home
/
Brands
/
Guidant Corporation Advanced CardiovascularSystem

Guidant Corporation Advanced CardiovascularSystem Recalls

All product recalls associated with Guidant Corporation Advanced CardiovascularSystem.

Get alerts for this brand

Recall Summary

Total Recalls

1000

Past Year

1000

Class I (Serious)

127

Most Recent

Jan 2026

Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.

Showing 24061–24080 of 25000 recalls

Guidant Corporation Advanced CardiovascularSystem: Voyager RX Coronary Dilatation Catheter

Leak at guide wire exit notch could introduce air into the artery.

FDAJan 27, 2005IN• Guidant Corporation Advanced CardiovascularSystem

AMF Support Surfaces Inc: Cool/Heat Versatility Main Controller Unit with 7-pin por...

Operator misconnected device power cords causing failure of the device.

FDAJan 27, 2005IN, MD, ND• AMF Support Surfaces Inc

Model 5101 Oil-Filled Heater (Lakewood) – Safety Concern (2005)

Fire/Burn Risk

The recalled heaters are portable electric radiator-style heaters with six fins, one of which has the control panel attached to it. The units are grayish-white in color and have the name "Lakewood" printed below the handle indentation on the control panel. The model number "5101" is printed on the UL label on the lower right side of the control panel.

1...1202 120312041205 1206...1250

Page 1204 of 1250Next

CPSCJan 26, 2005Nationwide• Lakewood Engineering and Mfg. Co., of Chicago, Ill.

GE OEC Medical Systems, Inc: InstaTrak 3500 Plus system with cranial application (aid ...

Tracking inaccuracy of 5-10 mm may result when the shunt guide accessory is used with version 5.1 software.

FDAJan 26, 2005AL, AK, AZ +21 more• GE OEC Medical Systems, Inc

ela Medical Llc: Sentinel Implantable Carioverter-DefibrilIator (ICD) mode...

A change in the automatic capacitor reform schedule during the later portion of the device's useful life can result in excessive 750V charge times and disable the device's ability to report an End of Life (EOL) indicator due to excessive charge times unless the patient is receiving periodic 750V therapy shocks.

FDAJan 25, 2005AZ, CA, GA +11 more• ela Medical Llc

Aprilaire Electronic Air Cleaners (Research Products) – Performance Issue (2005)

Fire/Burn Risk

The recall involves all Aprilaire Model 5000 Electronic Air Cleaners. The air cleaners are almond colored and are located near the heating and cooling equipment. An identification label on the access door reads "Aprilaire Model 5000."

CPSCJan 24, 2005Nationwide• Research Products Corp., of Madison, Wis.

Fun Years Music Big Drum Set (Kids Station) – Potential Injury (2005)

Choking Hazard

The recalled music set includes a yellow and green drum with a clear plastic lid and a red one-piece carrying strap that doubles as a storage and carrying case for additional instruments. The drum measures 12 inches in diameter and about 7.5 inches in height. The instruments stored in the drum include: purple drumsticks, yellow and red dumb-bell-shaped maracas, purple wrist bells, an orange recorder, a yellow harmonica, a red-rimmed tambourine and a yellow whistle. Only this musical set is part of this recall. A similar drum set sold at Toys "R" Us with a two-piece strap and different musical toys is manufactured by a different company and is not being recalled.

CPSCJan 19, 2005Nationwide• Kids Station Inc., of Miami, Fla., for Toys "R" Us, of Wayne, N.J.

North Coast Medi-Tek Inc: SourceOne Healthcare Technologies brand, Ultrasound Tray,...

Outside box labeling, containing 10 trays, incorrectly identified the product as ultrasound trays. Product is Breast Biopsy trays, Cat. 255826R2. Individual tray package labeling correctly identifies the product as Breast Biopsy tray.

FDAJan 18, 2005OH• North Coast Medi-Tek Inc

Millar Instruments, Inc: Mikro-Tip Disposable Angiographic Catheter manufactured b...

Wire braiding protruding from the catheter.

FDAJan 14, 2005CA, IN, MN +1 more• Millar Instruments, Inc

40-Watt Mini Spotlight Bulbs (Comtrad) – Fire Risk (2005)

Laceration Risk

The recalled 40-Watt "Type R" incandescent mini spot-light bulbs were included in two- and three-lamp accent lights in certain furniture hutch items manufactured by Sauder Woodworking Co. The furniture hutch models involved are: Model 9386 - Uses the three-lamp kit Model 9549 - Uses the two-lamp kit Model 9509 - Uses the two-lamp kit

CPSCJan 13, 2005Nationwide• Comtrad, Division of Waljon Ltd., Mississauga, Ontario, Canada

Mammut Barryvox Avalanche Transceivers – Technical Malfunction (2005)

The recalled Barryvoxes are 2004/2005 model Opto 3000 Avalanche Transceivers. The words, "Mammut" and "Barryvox" are printed on the front of the red and black transceivers. The serial numbers on the recalled units, which can be found in the battery compartment under the UPC code, include: M0080000 through M0088419, M0089616 through M0089800 and M0090000 through M0090419. The recalled units were shipped with an instructional CD and the box marked "Bonus CD Included." Units containing safe replacement transceivers have a red triangular label reading "New Casing" on the box.

CPSCJan 13, 2005Nationwide• Ascom Systec AG, Eichtal, of Switzerland

Radiometer America Inc: D7120, BG-OX Cartridge, D7120 REF 946-003, and 946-001, c...

QC Bias-a solution used in the manufacturing of the membrane had a different composition which introduces a bias of 20 mpH.

FDAJan 12, 2005Nationwide• Radiometer America Inc

LMS Medical Systems Ltd: CALM software, version 02.09.01 This software is intend...

A deficiency in the software code can, in certain circumstances, cause data for the wrong patient to be displayed in the Tracing Review screen when a user is acknowledging an Alert

FDAJan 11, 2005AL, IL, MD +2 more• LMS Medical Systems Ltd

Spacelabs Medical Incorporated: Ultraview Universal Clinical Workstation System Model 90385.

Weakness of the swivel base for the universal clinical workstation may result in the unit falling from its mounted position endangering users and patients.

FDAJan 7, 2005IN, OR• Spacelabs Medical Incorporated

Smiths Medical PM, Inc.: Advisor Vital Signs Monitor model 9200, catalog number 92...

An issue with the pace detect function was discovered on a 9200 II monitor. Could result in a falsely high or low heart rate reading.

FDAJan 5, 2005Nationwide• Smiths Medical PM, Inc.

Northwest Medical Physics Equipment Inc: ISOLOC Software Version 6.0, Part Number NT-NW-425-520. ...

When ISOLOC version 6.0 software was used in the Anatomic Landmark mode, the couch moves display in the Couch Translator window was incorrect.

FDADec 30, 2004Nationwide• Northwest Medical Physics Equipment Inc

General Electric Med Systems LLC: Precision 500D Radiographic/Fluoroscopic X-ray System, mo...

Units have a defect in accordance with 21 CFR 1003.2 because an incorrect exposure can occur.

FDADec 30, 2004Nationwide• General Electric Med Systems LLC

General Electric Med Systems LLC: Proteus XR/a Radiographic X-ray System, models 2259973-1,...

Units have a defect in accordance with 21 CFR 1003.2 because an incorrect exposure can occur.

FDADec 30, 2004Nationwide• General Electric Med Systems LLC

Diamedix Corporation: The Is-Legionella IgG/IgM/IgA test kits are packaged in c...

Laceration Risk

The kits belonging to lot #s 30804/30804Z and 91803Z may lose activity, after one or two usages, causing the OD values for the Cut-Off Calibrator and/or Positive Control to be recovered below their specified ranges.

FDADec 23, 2004Nationwide• Diamedix Corporation

Walther Air Pistols (Umarex) – Safety Risk (2004)

Fire/Burn Risk

The recalled air pistols include the Walther models CP Sport, CP99, and Nighthawk manufactured throughout 2003. The recalled models have a serial number of "J3," which is located on the right side of the air pistol. The Walther CP Sport and CP99 CO2 air pistols capture the look and feel of a Walther firearm. The Nighthawk air pistol is outfitted with a compensator, red dot sight, flashlight and a mounting system. If there is an asterisk inscribed next to the serial number, the air pistol is not part of the recall.

CPSCDec 22, 2004Nationwide• Umarex, of Arnsburg, Germany